For Application to Human Spaceflight and ISS Experiments: VESGEN Mapping of Microvascular Network Remodeling during Intestinal Inflammation.

Patricia Parsons-Wingerter, Hans-Christian Reinecker
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Abstract

Challenges to long-duration space exploration and colonization in microgravity and cosmic radiation environments by humans include poorly understood risks for gastrointestinal function and cancer. Nonetheless, constant remodeling of the intestinal microvasculature is critical for tissue viability, healthy wound healing, and successful prevention or recovery from vascular-mediated inflammatory or ischemic diseases such as cancer. Currently no automated image analysis programs provide quantitative assessments of the complex structure of the mucosal vascular system that are necessary for tracking disease development and tissue recovery. Increasing abnormalities to the microvascular network geometry were therefore mapped with VESsel GENeration Analysis (VESGEN) software from 3D tissue reconstructions of developing intestinal inflammation in a dextran sulfate sodium (DSS) mouse model. By several VESGEN parameters and a novel vascular network linking analysis, inflammation strongly disrupted the regular, lattice-like geometry that defines the normal microvascular network, correlating positively with the increased recruitment of dendritic cells during mucosal defense responses.

应用于载人航天和国际空间站实验:肠道炎症过程中微血管网络重构的VESGEN制图。
人类在微重力和宇宙辐射环境下进行长期太空探索和殖民所面临的挑战包括对胃肠道功能和癌症的风险知之甚少。尽管如此,肠道微血管的持续重塑对于组织活力、健康的伤口愈合以及成功预防或恢复血管介导的炎症或缺血性疾病(如癌症)至关重要。目前没有自动图像分析程序提供对粘膜血管系统复杂结构的定量评估,这是跟踪疾病发展和组织恢复所必需的。因此,通过血管生成分析(VESGEN)软件,从右旋糖酐硫酸钠(DSS)小鼠模型中发生肠道炎症的3D组织重建中绘制微血管网络几何形状异常的增加图。通过几个VESGEN参数和一种新的血管网络连接分析,炎症强烈地破坏了定义正常微血管网络的规则的、晶格状的几何结构,这与粘膜防御反应中树突状细胞募集的增加呈正相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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